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Fewer than 3% of the administered dose is excreted unchanged in urine. The connection involving dose and overall valproate concentration is nonlinear; focus will not maximize proportionally Along with the dose, but somewhat, increases into a lesser extent because of saturable plasma protein binding. The kinetics of unbound drug are https://landenncnzk.blog-a-story.com/14067894/getting-my-dapattoto-to-work

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